Visitor Monitoring Drug History: TAVIST
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: TAVIST
FDA Application No: (NDA) 017661
Active Ingredient(s): CLEMASTINE FUMARATE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for TAVIST, (NDA) 017661
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/11/2002 051Manufacturing Change or Addition  
6/6/1996 049Control Supplement  
10/31/1996 048New or Modified Indication  
10/20/1995 047Manufacturing Change or Addition  
10/17/1995 046Control Supplement  
11/7/1995 045Package Change  
6/8/1994 044Control Supplement  
2/3/1995 043Labeling Revision  
7/21/1994 042Control Supplement  
5/21/1993 041Package Change  
4/22/1993 040Control Supplement  
8/7/1992 038Labeling Revision  
7/22/1992 036Labeling Revision  
2/21/1991 035Control Supplement  
9/8/1992 034Control Supplement  
4/23/1992 033Control Supplement  
3/4/1991 032Control Supplement  
9/4/1992 031Package Change  
12/4/1987 030Control Supplement  
4/16/1986 028Control Supplement  
8/21/1992 026OTC Labeling  
4/15/1986 024Package Change  
3/1/1983 023Control Supplement  
7/15/1981 022Control Supplement  
7/17/1981 021Manufacturing Change or Addition  
5/1/1980 019Control Supplement  
4/1/1980 018Control Supplement  
4/17/1980 017Control Supplement  
4/20/1979 016Labeling Revision  
4/20/1979 015Control Supplement  
10/14/1980 014Control Supplement  
8/17/1978 013Control Supplement  
8/11/1978 012Control Supplement  
8/14/1978 011Labeling Revision  
8/14/1978 010Control Supplement  
5/30/1978 009Control Supplement  
5/30/1978 008Control Supplement  
5/24/1978 007Labeling Revision  
3/16/1979 006Labeling Revision  
3/16/1979 005General Efficacy (MarkIV)  
2/16/1978 004Labeling Revision  
2/16/1978 003Formulation Revision  
3/16/1979 002Formulation Revision  
2/25/1977 000Approval  
 
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